MEF2C haploinsufficiency syndrome: Report of a new MEF2C mutation and review
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference17 articles.
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2. Redefining the phenotype associated with MEF2C point mutations;Bienvenu;Neurogenetics,2013
3. Dravet syndrome – from epileptic encephalopathy to channelopathy;Brunklaus;Epilepsia,2014
4. Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion;Cardoso;Neurology,2009
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